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Details

Stereochemistry ACHIRAL
Molecular Formula C13H17N3O3S2
Molecular Weight 327.422
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYSOBUZOLE

SMILES

COC1=CC=C(C=C1)S(=O)(=O)NC2=NN=C(CC(C)C)S2

InChI

InChIKey=LZCBNYVJTNCPDR-UHFFFAOYSA-N
InChI=1S/C13H17N3O3S2/c1-9(2)8-12-14-15-13(20-12)16-21(17,18)11-6-4-10(19-3)5-7-11/h4-7,9H,8H2,1-3H3,(H,15,16)

HIDE SMILES / InChI

Molecular Formula C13H17N3O3S2
Molecular Weight 327.422
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Glysobuzole (stabinol) is a sulfonamide derivative with antihyperglycemic activity. Like sulfonylureas, glysobuzole is able to lower blood glucose levels by increasing the release of insulin from pancreatic beta cells.

Approval Year

PubMed

PubMed

TitleDatePubMed
Preliminary observations on management of diabetes with "stabinol".
1960 Sep 24
Patents

Sample Use Guides

Diabetes patients were started on four tablets of 250 mg (1 g) of stabinol (given in a single dose in the morning).
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:58:56 GMT 2023
Edited
by admin
on Sat Dec 16 16:58:56 GMT 2023
Record UNII
887VHL8899
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLYSOBUZOLE
INN   WHO-DD  
INN  
Official Name English
ISOBUZOLE
Common Name English
glysobuzole [INN]
Common Name English
Glysobuzole [WHO-DD]
Common Name English
BENZENESULFONAMIDE, 4-METHOXY-N-(5-(2-METHYLPROPYL)-1,3,4-THIADIAZOL-2-YL)-
Systematic Name English
8002 C. B.
Code English
STABINOL
Brand Name English
NSC-34014
Code English
N-(5-ISOBUTYL-1,3,4-THIADIAZOL-2-YL)-P-METHOXYBENZENESULFONAMIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29711
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
Code System Code Type Description
SMS_ID
100000084236
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
ChEMBL
CHEMBL1481457
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
INN
1195
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
NSC
34014
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
CAS
3567-08-6
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
WIKIPEDIA
Glysobuzole
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID0046276
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
NCI_THESAURUS
C65813
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
PUBCHEM
234310
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
EVMPD
SUB07958MIG
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
FDA UNII
887VHL8899
Created by admin on Sat Dec 16 16:58:56 GMT 2023 , Edited by admin on Sat Dec 16 16:58:56 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY